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VistaPano S Ceph 2.0 (VistaPano S Ceph) +3 more models
FDA 510(k)Class II (US FDA 510(k))
510(k) K240040
Identifiers
- 510(k) Number
- K240040 FDA 510(k)
- FDA Product Code
- MUH FDA 510(k)
- Models / Variants
- VistaPano S Ceph 2.0 (VistaPano S Ceph) FDA 510(k)VistaPano S 2.0 (VistaPano S) FDA 510(k)ProVecta S-Pan 2.0 (ProVecta S-Pan) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.1800 FDA 510(k)
- Regulation Number
- 872.1800 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
VistaPano S Ceph 2.0 (VistaPano S Ceph) +3 more models by Vatech Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 4 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K240040 | Class II | Active |
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Manufacturer
- Manufacturer
- Vatech Co., Ltd.
Sources (1)
- FDA 510(k) K240040 24 fields · synced Jun 18, 2026